Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
12	g.52676316C>G	CA16606335	KRT1	c.1434G>C (p.Glu478Asp) n.508G>C	ClinVar dbSNP
12	g.52676316C>A	CA217422	KRT1	c.1434G>T (p.Glu478Asp) n.508G>T	ClinVar dbSNP

Number of alleles fetched